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Inhomogeneity Based Characterization of Distribution Patterns on the Plasma Membrane

Cell surface protein and lipid molecules are organized in various patterns: randomly, along gradients, or clustered when segregated into discrete micro- and nano-domains. Their distribution is tightly coupled to events such as polarization, endocytosis, and intracellular signaling, but challenging t...

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Autores principales: Paparelli, Laura, Corthout, Nikky, Pavie, Benjamin, Wakefield, Devin L., Sannerud, Ragna, Jovanovic-Talisman, Tijana, Annaert, Wim, Munck, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5014321/
https://www.ncbi.nlm.nih.gov/pubmed/27603951
http://dx.doi.org/10.1371/journal.pcbi.1005095
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author Paparelli, Laura
Corthout, Nikky
Pavie, Benjamin
Wakefield, Devin L.
Sannerud, Ragna
Jovanovic-Talisman, Tijana
Annaert, Wim
Munck, Sebastian
author_facet Paparelli, Laura
Corthout, Nikky
Pavie, Benjamin
Wakefield, Devin L.
Sannerud, Ragna
Jovanovic-Talisman, Tijana
Annaert, Wim
Munck, Sebastian
author_sort Paparelli, Laura
collection PubMed
description Cell surface protein and lipid molecules are organized in various patterns: randomly, along gradients, or clustered when segregated into discrete micro- and nano-domains. Their distribution is tightly coupled to events such as polarization, endocytosis, and intracellular signaling, but challenging to quantify using traditional techniques. Here we present a novel approach to quantify the distribution of plasma membrane proteins and lipids. This approach describes spatial patterns in degrees of inhomogeneity and incorporates an intensity-based correction to analyze images with a wide range of resolutions; we have termed it Quantitative Analysis of the Spatial distributions in Images using Mosaic segmentation and Dual parameter Optimization in Histograms (QuASIMoDOH). We tested its applicability using simulated microscopy images and images acquired by widefield microscopy, total internal reflection microscopy, structured illumination microscopy, and photoactivated localization microscopy. We validated QuASIMoDOH, successfully quantifying the distribution of protein and lipid molecules detected with several labeling techniques, in different cell model systems. We also used this method to characterize the reorganization of cell surface lipids in response to disrupted endosomal trafficking and to detect dynamic changes in the global and local organization of epidermal growth factor receptors across the cell surface. Our findings demonstrate that QuASIMoDOH can be used to assess protein and lipid patterns, quantifying distribution changes and spatial reorganization at the cell surface. An ImageJ/Fiji plugin of this analysis tool is provided.
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spelling pubmed-50143212016-09-27 Inhomogeneity Based Characterization of Distribution Patterns on the Plasma Membrane Paparelli, Laura Corthout, Nikky Pavie, Benjamin Wakefield, Devin L. Sannerud, Ragna Jovanovic-Talisman, Tijana Annaert, Wim Munck, Sebastian PLoS Comput Biol Research Article Cell surface protein and lipid molecules are organized in various patterns: randomly, along gradients, or clustered when segregated into discrete micro- and nano-domains. Their distribution is tightly coupled to events such as polarization, endocytosis, and intracellular signaling, but challenging to quantify using traditional techniques. Here we present a novel approach to quantify the distribution of plasma membrane proteins and lipids. This approach describes spatial patterns in degrees of inhomogeneity and incorporates an intensity-based correction to analyze images with a wide range of resolutions; we have termed it Quantitative Analysis of the Spatial distributions in Images using Mosaic segmentation and Dual parameter Optimization in Histograms (QuASIMoDOH). We tested its applicability using simulated microscopy images and images acquired by widefield microscopy, total internal reflection microscopy, structured illumination microscopy, and photoactivated localization microscopy. We validated QuASIMoDOH, successfully quantifying the distribution of protein and lipid molecules detected with several labeling techniques, in different cell model systems. We also used this method to characterize the reorganization of cell surface lipids in response to disrupted endosomal trafficking and to detect dynamic changes in the global and local organization of epidermal growth factor receptors across the cell surface. Our findings demonstrate that QuASIMoDOH can be used to assess protein and lipid patterns, quantifying distribution changes and spatial reorganization at the cell surface. An ImageJ/Fiji plugin of this analysis tool is provided. Public Library of Science 2016-09-07 /pmc/articles/PMC5014321/ /pubmed/27603951 http://dx.doi.org/10.1371/journal.pcbi.1005095 Text en © 2016 Paparelli et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Paparelli, Laura
Corthout, Nikky
Pavie, Benjamin
Wakefield, Devin L.
Sannerud, Ragna
Jovanovic-Talisman, Tijana
Annaert, Wim
Munck, Sebastian
Inhomogeneity Based Characterization of Distribution Patterns on the Plasma Membrane
title Inhomogeneity Based Characterization of Distribution Patterns on the Plasma Membrane
title_full Inhomogeneity Based Characterization of Distribution Patterns on the Plasma Membrane
title_fullStr Inhomogeneity Based Characterization of Distribution Patterns on the Plasma Membrane
title_full_unstemmed Inhomogeneity Based Characterization of Distribution Patterns on the Plasma Membrane
title_short Inhomogeneity Based Characterization of Distribution Patterns on the Plasma Membrane
title_sort inhomogeneity based characterization of distribution patterns on the plasma membrane
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5014321/
https://www.ncbi.nlm.nih.gov/pubmed/27603951
http://dx.doi.org/10.1371/journal.pcbi.1005095
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